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dbVar

Database of genomic structural variation

nsv5927294

Organism: Homo sapiens

Study:nstd209 (Almarri et al. 2020)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:3,635

Publication(s):Almarri et al. 2020

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 215 SVs from 40 studies. See in: genome view

Submitted genomic31,675,993-31,679,627

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5927294	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000011.10	Chr11	31,675,993	31,679,627
nsv5927294	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000011.9	Chr11	31,697,541	31,701,175

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17358708	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17358708	Submitted genomic		NC_000011.10:g.316 75993_31679627del	GRCh38 (hg38)		NC_000011.10	Chr11	31,675,993	31,679,627
nssv17358708	Remapped	Perfect	NC_000011.9:g.3169 7541_31701175del	GRCh37.p13	First Pass	NC_000011.9	Chr11	31,697,541	31,701,175

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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